Canonical Allele Identifier: CA415009477
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12778250A>T , CM000686.2:g.12778250A>T GRCh38
NC_000024.9:g.14890184A>T , CM000686.1:g.14890184A>T GRCh37
NC_000024.8:g.13399578A>T NCBI36
NG_008311.1:g.82025A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2871A>T ENSP00000498372.1:p.Lys957Asn
ENST00000338981.7:c.2871A>T MANE Select ENSP00000342812.3:p.Lys957Asn
ENST00000426564.6:n.2883A>T
NM_004654.3:c.2871A>T NP_004645.2:p.Lys957Asn
XM_011531469.1:c.2871A>T XP_011529771.1:p.Lys957Asn
XM_011531470.1:c.2637A>T XP_011529772.1:p.Lys879Asn
XM_017030078.2:c.2886A>T XP_016885567.1:p.Lys962Asn
NM_004654.4:c.2871A>T MANE Select NP_004645.2:p.Lys957Asn